NM_000237.2:c.776-172G>A

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HGVS Expressions

  • NG_008855.2:g.58953G>A
  • NM_000237.2:c.776-172G>A
  • NP_000228.1:p.?
  • NC_000008.11:g.19955669G>A

Associated Genes

Lipoprotein Lipase
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

264

Clinvar

1282596

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.1United Arab EmiratesNA0.137AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 160 subjects with CAD from a study consi...
608320.G.2.2United Arab EmiratesNA0.086Osman et al. 2020 Group consisting of 332 control subjects...
608320.G.2.3United Arab EmiratesNAAssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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Contributors

  • Asha Deepthi: 07.09.2021

Edit History

  • Pratibha Nair: 21.11.2022
  • Rahila Mir: 03.02.2022
  • Asha Deepthi: 11.10.2021
  • Asha Deepthi: 29.09.2021
  • Asha Deepthi: 07.09.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.